| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:218097-218369 | Common:4; Rare:114; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr5:443074-443280 | Common:10; Rare:94 | ||||
| chr5:612203-612357 | Rare:61 | ||||
| chr5:693295-693520 | Common:5; Rare:69 | ||||
| chr5:892658-892947 | Common:5; Rare:99 | ||||
| chr5:1799785-1799988 | Common:7; Rare:96 | ||||
| chr5:1801295-1801460 | Common:4; Rare:82; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:5422334-5422689 | Common:2; Rare:116 | ||||
| chr5:6378505-6378699 | Rare:73 | ||||
| chr5:6633012-6633313 | Common:6; Rare:92; Clinvar:7; Clinvar (benign):2 | ||||
| chr5:7851082-7851210 | Common:1; Rare:21 | ||||
| chr5:7869000-7869200 | Common:2; Rare:100; Clinvar (benign):1 | ||||
| chr5:9546074-9546364 | Common:7; Rare:68 | ||||
| chr5:10249876-10250179 | Common:16; Rare:142 | ||||
| chr5:10250216-10250389 | Common:2; Rare:92; Clinvar:3; Clinvar (benign):2 |